Adjuvant therapy with oral fluoropyrimidines as main chemotherapeutic agents after curative resection for colorectal cancer: Individual patient data meta-analysis of randomized trials

被引:56
作者
Sakamoto, J [1 ]
Hamada, C [1 ]
Kodaira, S [1 ]
Nakazato, H [1 ]
Ohashi, Y [1 ]
机构
[1] Aichi Prefectural Hosp, Dept Surg, Okazaki, Aichi 444, Japan
关键词
adjuvant chemotherapy; colorectal cancer; 5-fluorouracil prodrugs; meta-analysis; oral; 5-fluorouracil; randomized clinical trials;
D O I
10.1093/jjco/29.2.78
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Oral 5-fluorouracil and its prodrugs (tegafur, carmofur) is now being studied for adjuvant chemotherapy of curatively resected colorectal cancers. To evaluate the effect of these oral fluoropyrimidines (o-FPs), an individual patient data (IPD) meta-analysis of randomized clinical trials was performed in Japan as an inter-trialist group study. Methods: Data from the three clinical trials in which postoperative adjuvant therapy with o-FPs was compared with surgery alone in patients with colorectal cancer were sought. IPD from a total of 4960 patients with follow-up periods of at least 5 years were analyzed. Results: The results of the meta-analysis on an 'intention to treat' basis demonstrated a significant benefit of o-FPs in terms of the disease-free survival (DFS) of the total patients [risk ratio (RR) 0.830, 95% confidence interval (CI) 0.742-0.929, P = 0.001]. o-FPs were also demonstrated to be effective far survival in rectal cancer (RR 0.857, 95% Ct 0.734-0.999, P = 0.049) and in Dukes'C colorectal cancer (RR 0.828, 95% CI 0.711-0.965, P = 0.016). Conclusion: The results suggest the advantage of long term o-FPs, possibly with the injection of mitomycin C, for prognosis for curatively resected colorectal cancer patients.
引用
收藏
页码:78 / 86
页数:9
相关论文
共 22 条
[1]  
ABE O, 1992, LANCET, V339, P71
[2]   CANCER STATISTICS, 1991 [J].
BORING, CC ;
SQUIRES, TS ;
TONG, T .
CA-A CANCER JOURNAL FOR CLINICIANS, 1991, 41 (01) :19-36
[3]  
BUYSE M, 1988, JAMA-J AM MED ASSOC, V259, P3571
[4]   ARE WE DOING BETTER WITH LARGE-BOWEL CANCER [J].
DECOSSE, JJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (12) :782-783
[5]  
*EARL BREAST CANC, 1992, LANCET, V339, P1
[6]   IMPORTANCE OF BETA, TYPE-II ERROR AND SAMPLE-SIZE IN DESIGN AND INTERPRETATION OF RANDOMIZED CONTROL TRIAL - SURVEY OF 71 NEGATIVE TRIALS [J].
FREIMAN, JA ;
CHALMERS, TC ;
SMITH, H ;
KUEBLER, RR .
NEW ENGLAND JOURNAL OF MEDICINE, 1978, 299 (13) :690-694
[7]  
GORGE SL, 1984, CANC CLIN TRIALS MET, P287
[8]  
Hanai A, 1998, JPN J CLIN ONCOL, V28, P54
[9]  
ITO K, 1996, P ASCO, V15, P24
[10]  
KASAI Y, 1995, JPN J CLIN ONCOL, V25, P91